Identification of potential causal variants for premature ovarian failure by whole exome sequencing

BACKGROUND: Premature ovarian failure (POF) is a highly heterogeneous disorder that occurs in 1% of women of reproductive age. Very few causative genes and variants contributing to POF have been detected, and the disease remains incompletely understood. In this study, we used whole exome sequencing...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:BMC Med Genomics
Egile Nagusiak: Jin, Haengun, Ahn, JuWon, Park, YoungJoon, Sim, JeongMin, Park, Han Sung, Ryu, Chang Soo, Kim, Nam Keun, Kwack, KyuBum
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: BioMed Central 2020
Gaiak:
Research Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC7590468/
https://ncbi.nlm.nih.gov/pubmed/33109206
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12920-020-00813-x
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